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DIACLON RH SUBGRUPOS + CW+K - INVIMA Registration 28aa107fc7c96fb41daecdd3eecce62f

Access comprehensive regulatory information for DIACLON RH SUBGRUPOS + CW+K (DIACLON RH SUBGRUPOS + CW+K) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 28aa107fc7c96fb41daecdd3eecce62f and manufactured by BIOCIENTIFICA LTDA.. The device was registered on May 23, 2029.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
III
28aa107fc7c96fb41daecdd3eecce62f
DIACLON RH SUBGRUPOS + CW+K
INVIMA Analysis ID: 28aa107fc7c96fb41daecdd3eecce62f
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Product Use / Uso del Producto
Spanish

ESTA TARJETA ID SIRVE PARA LA DETERMINACIร“N MANUAL_x000D_ Y EN INSTRUMENTOS DE LOS ANTรGENOS C (RH2), C (RH8),_x000D_ C (RH4), E (RH3), E (RH5) Y K (KEL1) EN ERITROCITOS _x000D_ HUMANOS. PARA LA UTILIZACIร“N EN SISTEMAS _x000D_ SEMIAUTOMATIZADOS O TOTALMENTE AUTOMATIZADOS _x000D_ CONSULTE ELMANUAL DE USUARIO CORRESPONDIENTE.

English

THIS ID CARD IS USED TO DETERMINE MANUAL_x000D_ AND IN INSTRUMENTS OF THE ANTIGENS C (RH2), C (RH8),_x000D_ C (RH4), E (RH3), E (RH5) AND K (KEL1) IN ERYTHROCYTES _x000D_ HUMAN. FOR USE IN _x000D_ SYSTEMS SEMI-AUTOMATED OR FULLY AUTOMATED _x000D_ PLEASE REFER TO THE RELEVANT USER MANUAL.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
28aa107fc7c96fb41daecdd3eecce62f
Expire Date
May 23, 2029
Authorized Company / Fabricante
Name (Spanish)
BIOCIENTIFICA LTDA.
Name (English)
BIOSCIENTIFIC LTDA.